Symbol Name ID |
Myo10
myosin X MGI:107716 |
Darker colors indicate more annotations |
Mouse Phenotypes | impaired pupillary reflex |
abnormal retina vasculature morphology |
abnormal eye morphology |
abnormal iris morphology |
iris coloboma |
abnormal cornea morphology |
cornea opacity |
fused cornea and lens |
abnormal lens morphology |
abnormal lens development |
cataract |
failure of eyelid fusion |
persistence of hyaloid vascular system |
microphthalmia |
abnormal retina morphology |
anophthalmia |
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Availability | Mouse Genotype | ||||||||||||||||
Myo10m1J/Myo10m1J | |||||||||||||||||
Myo10tm1a(KOMP)Wtsi/Myo10tm1a(KOMP)Wtsi | |||||||||||||||||
Myo10tm1d(KOMP)Wtsi/Myo10tm1d(KOMP)Wtsi | |||||||||||||||||
Myo10tm2(KOMP)Wtsi/Myo10tm2(KOMP)Wtsi |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/21/2024 MGI 6.24 |
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